MacNaul K L, Hutchinson N I
Merck Research Laboratories, Rahway, NJ 07065.
Biochem Biophys Res Commun. 1993 Nov 15;196(3):1330-4. doi: 10.1006/bbrc.1993.2398.
To examine the potential contribution of endothelial cell cNOS (ec-cNOS) and inducible NOS (iNOS) in controlling vascular tone under normal versus inflammatory conditions, we performed Northern hybridizations to examine the differential expression of each NOS mRNA in human aortic endothelial cells (AOEC) and human aortic smooth muscle cells (AOSMC) cultured for 8 h in the presence or absence of cytokines (IL-1 beta, TNF-alpha, and IFN-gamma) and LPS. Cytokine/LPS treatment induced a 4.4 kb iNOS mRNA in the human AOSMC; in contrast, cytokine/LPS treatment down regulated the expression of ec-cNOS mRNA in the AOEC. No iNOS mRNA was detected in the AOEC under the conditions examined. These results suggest that under specific inflammatory conditions the generation of NO in vascular tissue switches from ec-cNOS in the endothelium to iNOS in the smooth muscle.
为了研究在正常与炎症条件下内皮细胞型一氧化氮合酶(ec-cNOS)和诱导型一氧化氮合酶(iNOS)在控制血管张力方面的潜在作用,我们进行了Northern杂交,以检测在存在或不存在细胞因子(IL-1β、TNF-α和IFN-γ)及脂多糖(LPS)的情况下培养8小时的人主动脉内皮细胞(AOEC)和人主动脉平滑肌细胞(AOSMC)中各一氧化氮合酶mRNA的差异表达。细胞因子/LPS处理在人AOSMC中诱导产生了4.4 kb的iNOS mRNA;相反,细胞因子/LPS处理下调了AOEC中ec-cNOS mRNA的表达。在所检测的条件下,AOEC中未检测到iNOS mRNA。这些结果表明,在特定的炎症条件下,血管组织中一氧化氮的产生从内皮中的ec-cNOS转变为平滑肌中的iNOS。